Idiopathic dilation cardiomyopathy
Dilated cardiomyopathy that is characterized by cardiac dilatation and reduced systolic function. It is the most frequent form of cardiomyopathy and accounts for more than half of all cardiac transplantations performed in children between 1 and 10 years of age. For CMD1A, 20 to 30% of cases are heritable and show an autosomal dominant inheritance pattern. Germline mutations in the LMNA gene have been identified. OMIM: 115200
Also Known As:
Cardiomyopathy, Dilated, 1h; Cardiomyopathy, Dilated, With Conduction Defect; Dilated cardiomyopathy with conduction defect
Networked: 2
relevant articles (0 outcomes,
0 trials/studies)
Disease Context: Research Results
Related Diseases
Experts
1. | Dubbioso, Raffaele:
1 article
(04/2015)
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2. | Fiorillo, Chiara:
1 article
(04/2015)
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3. | Iodice, Rosa:
1 article
(04/2015)
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4. | Manganelli, Fiore:
1 article
(04/2015)
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5. | Ruggiero, Lucia:
1 article
(04/2015)
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6. | Santorelli, Filippo:
1 article
(04/2015)
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7. | Santoro, Lucio:
1 article
(04/2015)
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8. | Soscia, Ernesto:
1 article
(04/2015)
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9. | Storti, Eugenia:
1 article
(04/2015)
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10. | Tessa, Alessandra:
1 article
(04/2015)
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Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Idiopathic dilation cardiomyopathy: